rs1057519292
A SNP in the ATP13A2 gene on chromosome 1. Its most notable genotype is A;A: Spastic paraplegia, type 78
- Gene
- ATP13A2
- Location
- Chr 117,004,805 (GRCh38)
- Highest magnitude
- 7.8Very important
- Tested on
- Not on consumer chips
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon/normal
- A;GBadCarrier of a spastic paraplegia mutation (type 78)
- A;AMost notableBadSpastic paraplegia, type 78
SNPedia records rs1057519292 on the minus strand: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other ATP13A2 SNPs
- rs121918227G;GParkinson's mutation, type 9, early-onsetVery important
- rs144701072T;TParkinson's mutation, type 9, early-onsetVery important
- rs199624796A;AParkinson's mutation, type 9, early-onsetVery important
- rs587776890-;-Parkinson's mutation, type 9, early-onsetVery important
- rs587777053G;GParkinson's mutation, type 9, early-onsetVery important
- rs749798211-;-Parkinson's mutation, type 9, early-onsetVery important
- rs762033589TC;TCParkinson's mutation, type 9, early-onsetVery important
- rs786205056T;TParkinson's mutation, type 9, early-onsetVery important
Notes
From SNPedia
Notes
c.364C>T (p.Gln122Ter)
A;G
see ATP13A2
A;A
see ATP13A2
Source and license
Adapted from rs1057519292 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.